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  • 1970-1974  (10,782)
  • Polymer and Materials Science  (10,782)
  • 201
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 18 (1974), S. 93-103 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: A study has been carried out of the relationship between polymer orientation and dyeing behavior using a specially prepared range of nylon 66 samples varying only in orientation and five dyes normally showing varying degrees of sensitivity to physical variations in nylon. Integral diffusion coefficients have been calculated using Crank's finite dyebath equation from appropriate rate of dyeing data. Evidence has been produced which suggests that except with dyes of low molecular weight, i.e., dyes insensitive to physical variations in the nylon, a diffusional interaction between diffusing dye molecules exists which leads to a variation in the concentration dependence of the diffusion coefficient with fiber orientation. The length of the diffusing dye ion has been shown to be of decisive importance in this interaction.
    Additional Material: 5 Ill.
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  • 202
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    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 18 (1974), S. 3685-3697 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Molecular weights from GPC curves are determined for EPM, EPDM, and some polybutadienes. The determinations make use of a Benoit factor, B, which is defined and tabulated for the polymers studied. The use of this factor provides a convenient method of employing the Benoit hypothesis. The Mn from the GPC curves are compared with osmotic molecular weights to provide additional confirmation of the Benoit hypothesis. The Mv from the GPC curves are used with intrinsic viscosity data to establish [η]-versus-M relations.
    Additional Material: 1 Ill.
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  • 203
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    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 18 (1974), S. 3731-3738 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The sorption kinetics of p-nitrophenol (PNP) onto undrawn nylon yarn from an organic, nonswelling solvent in a dye bath in which the concentration of PNP was being depleted were found to obey Hill's solution of the diffusion equation, suggesting the presence of a monolayer of absorbed PNP at the surface of the fiber. Diffusion coefficients were obtained using a nonlinear least-squares curve-fitting computer program. For undrawn nylon samples, oxidized for various lengths of time prior to dyeing, the diffusion coefficient increased as a function of oxidation time, rising particularly rapidly once the fibers developed microscopically visible surface cracks. The dependence of diffusion coefficient on oxidation time implies that oxidative degradation of the material is accompanied by formation of submicroscopic incipient cracks, permeable by PNP, of which at least some eventually develop into visible cracks after sufficient oxidation.
    Additional Material: 2 Ill.
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  • 204
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    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 18 (1974), S. 3769-3773 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Additional Material: 2 Ill.
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  • 205
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    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science: Macromolecular Reviews 8 (1974), S. 1-49 
    ISSN: 0076-2083
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 2 Ill.
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  • 206
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    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science: Macromolecular Reviews 8 (1974), S. 51-115 
    ISSN: 0076-2083
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 207
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    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science: Macromolecular Reviews 9 (1974), S. 127-162 
    ISSN: 0076-2083
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 9 Ill.
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  • 208
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    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 18 (1974), S. 21-43 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The adhesion between ammonium perchlorate filler and the polybutadiene rubber matrix was investigated. The aggregate composite was modified by surface pretreatment of the filler with various organofunctional silanes. For comparison, the adhesion of glass beads and glass powder, each coated with a fluorocarbon release agent, and carbon black were used as fillers in the cured polybutadiene matrix. Common testing methods used included the determination of Poisson's ratio, photographic analysis, and absorption of water. A new type of stress-strain analysis was introduced. Results closely agreed with established composite theory. The presence of methacryloxy- and amino-functional silanes improved adhesion to the resin system. Epoxy- and vinyl functional silanes proved to be detrimental at the filler-rubber interface. A major function of the coupling agents appears to be to eliminate the weak boundary layer of surface moisture on the filler particles.
    Additional Material: 18 Ill.
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  • 209
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    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 18 (1974), S. 61-75 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The viscosity of concentrated (17.5 g/dl) solutions of cellulose acetate in 11 single solvents and in four binary solvent mixtures was related to a thermodynamic measure of solvent power. In single solvents, the specific viscosity varied from 4600 in dimethyl sulfoxide to 78,000 in diacetone alcohol, with the specific viscosity increasing with decreasing abolute value of the partial molar free energy of dilution. This behavior can be accounted for by the hypothesis that the number of chain entanglements increases with decreasing solvent power. In solvent mixtures, the specific viscosity often attains a minimum value at a composition where the average solubility parameter locus is near the center of the solubility region of the polymer.
    Additional Material: 6 Ill.
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  • 210
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    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 18 (1974), S. 117-124 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The efficiency of three commercial ultraviolet absorbers, a 2-hydroxy benzophenone, a 2-hydroxy benzotriazole, and a nickel chelate, in preventing the photo-oxidation of polystyrene films has been measured. When compared with the calculated screening and phosphorescence quenching efficiency, it is found that (i) the nickel chelate protects the substrate by UV screening alone and is a poor photoprotector, and (ii) the 2-hydroxy benzophenone and 2-hydroxy benzotriazole are more efficient photoprotectors and protect by triplet energy transfer from excited polymer carbonyl impurity groups in addition to UV screening.
    Additional Material: 2 Ill.
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  • 211
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    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 18 (1974), S. 155-165 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The structure of polyethylenimine in aqueous and ethanolic solutions was investigated by measuring the fluorescence polarization of dansyl conjugates. In aqueous solutions, all polyethylenimines, whatever their molecular weight, are associated into large aggregates containing rotating units having rotary relaxation times corresponding to spherical particles of molecular weight about 3-6 × 103. The interaction of polyethylenimine with very dilute solutions of linear high polymers has been investigated by fluorescence polarization measurements and by the measurement of turbulent drag. Addition of polyethylenimine causes the solutions of anionic polymers to lose their capability of reducing turbulent drag. The results are discussed in relation to the proposed structure of the anionic-cationic complexes formed in the mixtures.
    Additional Material: 2 Ill.
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  • 212
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    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 18 (1974), S. 245-255 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Polystyrene test pieces broken by flexure in the presence of n-propanol and other alcohols have been examined by scanning electron microscopy. Two regions on the fracture surface are observed; a narrow band near to the tension surface corresponds to fracture through a solvent craze, but the remainder of the surface is identical to fracture surfaces produced in air. The solvent-crazed region has a cellular structure decreasing in scale toward the tip of the craze. An explanation of these features is offered in terms of the changing conditions of stress and solvent content ahead of the growing craze.
    Additional Material: 11 Ill.
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  • 213
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    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 18 (1974), S. 379-388 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The possibility of eliminating sodium alkylbenzenesulfonate (ABS) from water by reverse osmosis was examined by operating with polypropylene membranes grafted with poly(acrylic acid). Flux through the membranes decreases with increasing thickness. For 23μ thickness and 0.5 1./hr-m2 flux, the rejection is 100% (operating pressure, 50 atm: concentration, 1 g ABS/l.). For 5μ thickness the rejection is lower and is related to ABS concentration: rejection increases with increasing concentration and reaches 60% for concentrations higher than 5 g ABS/l. (flux, 51./hr-m2; operating pressure, 50 atm). This is ascribed to the prevailing ultrafiltration as regards the reverse osmosis. ABS, at higher concentrations than the critical value, gives micelles whose dimensions might be compared to pores. The membrane behavior is influenced by previous treatments; when the membrane has been conditioned in NaCl solution, it is more selective and more permeable; the rejection reaches 90% with fluxes of 6.8 l./hr-m2 for concentrations of 5 g ABS/1. (operating pressure, 50 atm). In order to relate the properties to the structure of membranes, we have examined them by electron microscope. The ion exchange which takes place between membrane and NaCl and between membrane and ABS has also been studied.
    Additional Material: 8 Ill.
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  • 214
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    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 18 (1974), S. 439-448 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Poly-p-xylylene and three halogen-containing poly-p-xylylenes prepared by the Gorham method from purified dimers were characterized by thermogravimetry and differential scanning calorimetry to determine their relative thermal stabilities in nitrogen and air. As judged by these techniques, thermal stability in nitrogen is not greatly changed by halogenation of the cyclic dimer from which polymer is made. However, thermal oxidative stability depends on the type and degree of halogenation. Aliphatic fluorine atoms greatly improved upon the thermal oxidative stability of poly-p-xylylene. To a lesser but significant degree, two aromatic chlorine atoms, poly(dichloro-p-xylylene), also improved upon the thermal oxidative stability of poly-p-xylylene or poly-(chloro-p-xylylene). Oxidative degradation caused a rapid exothermic weight loss near 300°C for poly(dichloro-p-xylylene) and near 250°C for poly-p-xylylene and poly(chloro-p-xylylene) when films were heated at 10°C/min. Poly(dichloro-p-xylylene) maintained a constant weight during an induction period before it started to lose weight when it was heated isothermally at temperatures below 300°C. However, poly-p-xylylene and poly(chloro-p-xylylene) gained weight during oxidation before they lost weight when heated isothermally below 250°C.
    Additional Material: 8 Ill.
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  • 215
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Grafting of chain-growth polymerizable monomers onto cellulose has been a thoroughly investigated area. Introduction of polymerizable monomeric species chemically bound to cellulose has been less fruitful. Crotonate esters, methacrylate esters, and allyl and vinyl derivatives are examples where subsequent polymerization to crosslinked species has been described. Reported are the reactions of vinylbenzyl chloride with causticized cotton fabric to give a series of vinylbenzylated celluloses with degrees of substitution from 0.05 to 0.26. Homopolymerization of these or copolymerization with maleic anhydride or dimethyl maleate gave little or no crosslinking under the conditions employed. Vinylbenzyl cellulose acetate proved to be a polymerizable “prepolymer” with diethyl maleate.
    Additional Material: 12 Ill.
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  • 216
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    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 18 (1974), S. 689-698 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Two-component interpenetrating polymer networks (IPN) of the SIN type (simultaneous interpenetrating networks) were prepared from three different polyurethanes and two epoxies. The linear prepolymers were combined in solution, together with crosslinking agents and catalysts, films cast, and subsequently chain extended and crosslinked in situ. Two of the IPN's showed significant improvement in thermal resistance, as measured by thermogravimetric analysis (TGA). All of the IPN's showed maxima in tensile strength significantly higher than the tensile strengths of the component networks at 25% polyurethane and minima at 75% polyurethane. The minima were explained by an initial dilution of the strong polyurethane hydrogen bonds by the epoxies, and the maxima, by an increase in crosslink density due to interpenetration.
    Additional Material: 8 Ill.
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  • 217
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    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 18 (1974), S. 745-752 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: A number of organotin compounds of the type RnSn Y4-n, where R = alkyl or aryl; Y = alkylthio, arylthio or carbothiolate; and n = 1, 2, 3 have been prepared and treated with hydrogen chloride at 180°C in o-dichlorobenzene solution. The organotin compounds were also tested at 190°C as thermal stabilizers for PVC. Cleavage of tin-carbon bonds by hydrogen chloride was demonstrated in some cases by analysis of the organotin-hydrogen chloride reaction products. The formation of monoalkyl(aryl)tin chlorides or stannic chloride, or both, in the model system was shown to correspond to a catastrophic mode of degradation in the polymer. The use of stabilizers with fewer than two alkyl or aryl groups on tin also gave this mode of degradation.
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  • 218
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    Journal of Applied Polymer Science 18 (1974), S. 805-819 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Pore sizes of microporous polymer membranes were determined by the calculation based on the gas permeability of porous media. The gas permeability coefficient K (given by J = K Δp/l, where J is the steady-state gas flux, Δp is the pressure, difference, and l = the thickness of a membrane) for porous membrane can be given generally by \documentclass{article}\pagestyle{empty}\begin{document}$$ K = K_0 + \frac{{B_0 }}{\eta }\Delta \bar p $$\end{document} where K0 is the Knudsen permeability coefficient, η is the viscosity of the permeant gas, B0 is the geometric factor of a membrane, and Δp̄ is the mean pressure of the gas on both sides of a membrane. From gas permeability measurements which yield the pressure dependence of gas permeability coefficient (expressed as above equation), the mean pore size of the porous membrane can be estimated as \documentclass{article}\pagestyle{empty}\begin{document}$$ m = \left( {\frac{{B_0 }}{{K_0 }}} \right)\left( {\frac{{16}}{3}} \right)\left( {\frac{{2RT}}{\pi }} \right)^{{\raise0.7ex\hbox{$1$} \!\mathord{\left/ {\vphantom {1 2}}\right.\kern-\nulldelimiterspace} \!\lower0.7ex\hbox{$2$}}} M^{ - {\raise0.7ex\hbox{$1$} \!\mathord{\left/ {\vphantom {1 2}}\right.\kern-\nulldelimiterspace} \!\lower0.7ex\hbox{$2$}}} $$\end{document} where M is the molecular weight of the permeant gas. The validity of this method was examined with various Millipore filters of which nominal pore sizes are known. It was confirmed that the method provided a simple and reliable means of estimating mean pore size of microporous membranes. The method was applied to investigate the influence of factors involved in preparation of microporous polysulfone membranes by coagulation procedure. It was found that the mean pore size of porous polysulfone membrane increases with (1) increasing with casting thickness, (2) increasing temperature of coagulation bath, and (3) decreasing concentration of polymer in casting solution (DMF as solvent). Water flux and water flux decline due to compaction are also examined as a faction of pore size, porosity, and the thickness of membranes.
    Additional Material: 7 Ill.
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  • 219
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    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 18 (1974), S. 857-865 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Polystyrene has been fractured in tension at two temperatures in n-heptane and n-propanol and the fracture surfaces studied by optical and scanning electron microscopy. The test temperatures were selected such as to be approximately 20°C above and below the temperatures at which it was expected1 that a glass-to-rubber transition would occur in the solvent-penetrated craze material. It was found that features of the fracture process and also structure of the fracture surfaces were different at the two temperatures. These changes have been interpreted in terms of a Tg occurring in the craze material.
    Additional Material: 6 Ill.
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  • 220
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    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 18 (1974), S. 925-931 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The method of Hamielec and Ray for correcting GPC molecular averages is discussed. It is shown that this method can be combined with the resolution index concept of Smith and Feldman to provide a simple accurate correction method. Practical application of the method to four different column combinations is discussed. Three of the combinations are typical Styragel column combinations, and they are very similar in their correction requirements. The fourth combination employed less gel with resultant higher flow rates and much shorter residence times. It required a larger correction factor, but even so, only a 17% correction to the weight-average or number-average molecular weight was required.
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  • 221
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    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 18 (1974), S. 943-946 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Additional Material: 1 Ill.
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  • 222
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    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 18 (1974), S. 947-949 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Additional Material: 2 Ill.
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  • 223
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    Journal of Applied Polymer Science 18 (1974), S. 939-941 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Additional Material: 3 Ill.
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  • 224
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    Journal of Applied Polymer Science 18 (1974), S. 1039-1042 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: “Replica gel” polymers, characterized by their extremely high specific surface area, have not previously been prepared in “redox” form. Some illustrative syntheses are described, and the capability of these materials to oxidize acetic acid and to epoxidize oleic acid and cyclohexene is demonstrated.
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  • 225
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    Journal of Applied Polymer Science 18 (1974), S. 1079-1082 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The crosslink density of small microtomed samples of rubber vulcanizates has been determined using a gas-chromatographic method for estimating the amount of solvent in the swollen rubber. The method may be used for determining the variation in crosslink density through thick rubber articles, for determining the change in crosslink density after aging service, or, for the investigation of rubber bonds and interfaces.
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  • 226
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    Journal of Applied Polymer Science 18 (1974), S. 1117-1130 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The chemical structure and cure characteristics of a group of phenolic resole resins were studied by means of three major analytical techniques. In particular, the effects on structure and reactivity of formaldehyde/phenol ratio and the type of reaction catalyst used were studied. Gel permeation chromatography was used to determine resin molecular weight distributions, and NMR, to determine chemical structural features. In this connection a selective oxidation procedure, converting free methylol groups to adehydes, has allowed unambiguous determination of methylene ether bridge structures to be made from the NMR data. The F/P ratio in a resole largely determines the type of molecular structures which are formed. However, triethylamine as a catalysts tends to favor methylene ether bridge formation, whereas sodium hydroxide favors methylene bridges. The rate and direction of subsequent thermal cure of the resoles prepared is shown by differential scanning calorimetry to depend markedly on the type of catalyst present during the curing stage. The DSC curing curves are interpreted in the light of the structural information provided by NMR.
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  • 227
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    Journal of Applied Polymer Science 18 (1974), S. 1269-1277 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The use of Cobalt(II) complexed with various polyaminocarboxylic acids and hydrogen peroxide has been shown to be an effective initiator for the emulsion polymerization of styrene. The polyaminocarboxylic acids used were ethylenediaminetetraacetic acid (EDTA), ammonia diacetic acid (ADA), N,N′-bis(2-aminoethyl)ethylenediaminehexaacetic acid (TTHA), ammonia triacetic acid (ATA), and N′-hydroxyethylethylenediamine-N,N,N′-triacetic acid (HEEDTA). In the case of the HEEDTA system, the effect of varying the concentrations of the initiator components was examined and found to be broadly similar to that observed in other metal ion chelate-hydrogen peroxide initiators. All the systems were effective over a wide pH range (generally 3-9), and zero-order rates in the range of 30-90%/hr were observed, although there was considerable variation in detail in the manner in which the zero-order rate depended on pH. The behavior of these systems is commented upon in the light of earlier results on similar systems and of previously published redox potentials of the related cobalt(II)-cobalt(III) chelate systems.
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  • 228
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    Journal of Applied Polymer Science 18 (1974), S. 1319-1350 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Fracture response of polyimide and polysulfone in tension under superimposed hydrostatic pressures up to 100,000 psi is presented. The influence of hydrostatic pressure and the pressure medium on the specific surface energy γ is determined by utilizing the Griffith theory of brittle fracture. For polyimide as well as for polysulfone, γ is found to increase with increasing pressure. Furthermore, for polysulfone at any given pressure level, the value of γ is found to be lower in heptane medium than in kerosene. Heptane is known to be a stress-cracking agent for polysulfone. Fracture surface of the tested tensile specimens is examined by using a scanning electron microscope. The observed fracture features are correlated with the macroscopic deformation behavior and also with the effects of the pressure medium used. In polyimide, the region of crack initiation narrows down from a very broad region at atmospheric pressure to almost a point source along the outer periphery of the specimen at 100,000 psi. In addition, polyimide undergoes a transition in the nature of fracture response between 80,000 to 100,000 psi, and this is clearly indicated in the scanning electron micrographs. In polysulfone, the crack propagation appears to be faster when heptane is used as the pressure medium than when kerosene is used. The penetration of the medium into the specimens can be observed on the micrographs. Several scanning electron micrographs of the fracture surface suggest the possibility of a significant temperature rise in the specimen during fracture. This increase in the specimen temperature is roughly estimated from the stored elastic energy released upon fracture.
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    Journal of Applied Polymer Science 18 (1974), S. 1385-1396 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Computer programs were developed to produce graphic plots which simulate the lowangle x-ray scattering curves obtained from cast films of triblock copolymers. Models were developed to take account of lattice paracrystallinity, a distribution in size of the scattering elements, various types of lattice packing, and the possibility of more than one type of lattice packing in a loosely bound paracrystal. These studies provide an insight into the possible structure of the macrolattices which have been observed with triblock copolymers.
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  • 230
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    Journal of Applied Polymer Science 18 (1974), S. 1423-1431 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Monomeric formaldehyde and the cyclic oxymethylenes tetraoxane and pentaoxane were retained by cotton to similar extents at the high temperatures used in textile finishing, but the mechanisms of absorption appeared to differ. Trioxane, however, was not retained by cotton. The absorption of cyclic oxymethylenes did not seem to involve bonding to cellulose by primary valence bonds. The presence of other substances had a greater effect on the absorption of monomeric formaldehyde than of cyclic oxymethylenes, but changes in extent of absorption were not large enough to influence textile properties of treated fabric.
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  • 231
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    Journal of Applied Polymer Science 18 (1974), S. 1451-1476 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Molecular motions in several polyblends and composites based on bisphenol A polycarbonate were investigated over a wide temperature range by means of two pulsed nuclear magnetic resonance methods: the spin-lattice relaxation time T1 and the spin-lattice relaxation time in rotating frame T1ρ. Characteristic changes in the transitions of the polyblends and composites with respect to the transitions of unmodified homopolymers and copolymers were observed. By selecting different types and quantities of materials to modify the matrix (bisphenol A polycarbonate) these changes were analyzed. It was found that the multiple transitions in the composites and polyblends were not always combinations of the transitions present in the constituent materials, but depended on compatibility of the polymers and the type of molecular motions of the individual components. Unlike other methods of investigating polymers in bulk, nuclear magnetic relaxation methods are sensitive to supramolecular structure or morphology. Supplemented with transmission and scanning electron micrographs, the results from these experiments led to the postulation of interaction domains or zones between the two phases in certain nonhomogeneous polymer systems in which the motions in one phase (usually the continuous phase) were affected by the motions in the other phase (usually the dispersed phase). Information on the nature and extent of this interaction was obtained by the NMR relaxation methods. The experimental results reflect not only the presence of separate phases in the nonhomogeneous materials, but also the complex heterogeneity of such systems. The results suggest correlations between internal molecular motions and physical properties of the materials examined. Based on the above concepts, a mechanism of rubber reinforcement was proposed. The impact strength of a rubber-modified polymer is related to the apparent volume of the rubber phase. This volume consists of the actual volume of the rubber plus the affected portion of the surrounding glassy matrix which, assisted by the segmental motions of the rubber, assumes the same motions.
    Additional Material: 20 Ill.
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  • 232
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    Journal of Applied Polymer Science 18 (1974), S. 1773-1778 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Polyurethane prepared from tetramethylene glycol and diisocyanate was exposed in the form of films to small pressures of NO2 and to NO2 plus air. Tensile strength was measured as a function of exposure time and temperature with an apparatus especially constructed for the purpose of measuring mechanical properties in different environmental “atmospheres.”
    Additional Material: 7 Ill.
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  • 233
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    Journal of Applied Polymer Science 18 (1974), S. 389-399 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Kinetics of heterogeneous oxidation of starch with hypochlorite were studied under varying conditions of temperature, pH, buffer components, buffer concentration, and concentration of substrate and oxidant. The kinetic data show that the reaction is first order with respect to hypochlorite. A plot of first-order rate constant for varying starch concentrations versus starch concentration is linear. The rate of oxidation of starch is highest at pH 7.0 and decreases with increasing acidity or alkalinity of the medium. In unbuffered system, pH of the medium decreases from 10 to 3.4 during the reaction. Based on observed trends of reaction rate, energy, and entropy of activation, a mechanism for hypochlorite oxidation of starch is proposed.
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  • 234
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    Journal of Applied Polymer Science 18 (1974), S. 1927-1942 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Gel permeation chromatography of polyoxymethylene has been studied using N,N-dimethylformamide as the solvent. Polyoxymethylene samples used here are a copolymer of tetraoxane with 1,3-dioxolane and a commercial polyoxymethylene whose molecular weight distributions are moderately broad. Their intrinsic viscosities [η] range from 1.4 to 2.8 dl/g. Factors affecting chromatograms are discussed, and the operating conditions were determined by using the analytical scale GPC. On the basis of these operating conditions, the molecular weight fractionation of polyoxymethylene was carried out by using the preparative scale GPC. It was found that polyoxymethylene can be effectively fractionated to give seven to ten fractions each of them containing the fractionated polymer ranging in weight from 0.2 to 8 mg when 40 mg polymer sample was used for a run of the measurement. The fractionated polymers were also found to have a narrow molecular weight distribution within a single peak, and their Mw/Mn values decrease with increasing molecular weight.
    Additional Material: 14 Ill.
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  • 235
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    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: On complete hydrazinolysis of poly(ethylene terephthalate), terephthalomonohydrazide is formed from carboxyl-end terephthaloyl residues in a quantity equivalent to the content of carboxyl endgroups in the polymer. The compound is separated from the reaction mixture by ion exchange and determined photometrically [epsiv;240 in 0.1 N HCl = 16,700 (1000 cm2/mole)]. A COOH determination carried out in this way is endgroup specific and, unlike titration, is not subject to interference by ionogenic fiber additives. Aromatic comonomers with acidic substituents (e.g., 5-sulfoisophthalic acid) in chemically modified, cationically dyeable poly(ethylene terephthalate) are determined simultaneously with the carboxyl endgroups by the same analytical method. In this case, the terephthalamonohydrazide and 5-sulfoisophthalodihydrazide are separated by ion exchange, and the difference in their spectral behavior is used for quantitative determination with the aid of a two-component analysis: \documentclass{article}\pagestyle{empty}\begin{document}$$ \begin{array}{l} c_1 {\rm = (6}{\rm .21 }D_{240} {\rm - 1}{\rm .04 }D_{212} ){\rm } \times {\rm 10}^{{\rm - 5}} {\rm mole/l}{\rm .} \\ c_2 {\rm = (2}{\rm .62 }D_{212} {\rm - 0}{\rm .51 }D_{240} ){\rm } \times {\rm 10}^{{\rm - 5}} {\rm mole/l} \\ \end{array} $$\end{document} where c1c2 = concentration of terephthalomonohydrazide and 5-sulfoisophthalodihydrazide, respectively; and D240 D212 = optical density at 240 and 212 nm, respectively. The content of carboxyl endgroups in polyether esters poly(p-(2-ethyleneoxy)-benzoate), is determined on the basis of the p-(β-hydroxyethoxy)benzoic acid [epsiv;258 in 0.1 N HCl = 16,100 (1000 cm2/mole)] liberated from carboxyl-end monomer units by hydrazinolysis. For copolyether esters with p-(β-hydroxyethoxy)benzoic acid as a comonomer, the contents of carboxyl-end terephthalic acid and p-(β-hydroxyethoxy)benzoic acid are determined simultaneously with the acid of a spectrophotometric twocomponent analysis: \documentclass{article}\pagestyle{empty}\begin{document}$$ \begin{array}{l} c_1 {\rm = (7}{\rm .65 }D_{240} {\rm - 3}{\rm .27 }D_{258} ){\rm } \times {\rm 10}^{{\rm - 5}} {\rm mole/l}{\rm .} \\ c_2 {\rm = (7}{\rm .91 }D_{258} {\rm - 3}{\rm .49 }D_{240} ){\rm } \times {\rm 10}^{{\rm - 5}} {\rm mole/l.} \\ \end{array} $$\end{document} where c2, c2 = concentration of terephthalomonohydrazide and p-(β-hydroxyethoxy)-benzoic acid, respectively; and D240, D258 = optical density at 240 and 258 nm, respectively.
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    Journal of Applied Polymer Science 18 (1974), S. 2039-2045 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Local strain disturbances near a running crack in a viscoelastic material were investigated in PMMA. Specimens having different initiation crack tip radii and under different tensile strain rates were examined by use of a series of strain gauges placed parallel and close to the expected crack path, and by velocity gauges. The strain disturbance, which was observed ahead of the running crack front, diminished gradually owing to the viscoelastic damping. The maximum strain disturbances increased with increase in gross breaking load.
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  • 237
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    Journal of Applied Polymer Science 18 (1974), S. 2069-2073 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The application of an oligomer as an internal standard in gel permeation chromatography was studied on narrow low molecular weight fractions of linear polyethylene using n-decane as the standard. A Waters gel permeation chromatograph was run continuously at 130°C with 0-dichlorobenzene as solvent. It has been found that the values of the elution volume of given samples vary with time and that a simple correction using n-decane as an internal standard reduces the inaccuracy from the original 6% to less than 1%. The corrected elution volumes remain reproducible over a period of several months so that frequent calibration is eliminated. The use of the oligomer chemically similar to the polymer samples gives a much better result than the use of low molecular weight impurity as the standard.
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  • 238
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    Journal of Applied Polymer Science 18 (1974), S. 2149-2163 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The surface concentration of polymer molecules in solution has been combined with the three-component bulk-phase diagram of Strathmann et al. to describe the complete equilibrium thermodynamic precasting situation. The polymer surface concentration is estimated according to the theory of Prigogine and Marechal as used by Siow and Patterson, and is governed by the relative values of the polymer and solvent surface tension, γp and γs respectively. In general, when γp 〉 γs, the cast membrane will tend to form with the asymmetric layer on the support side; for γp 〈 γs it will tend to form on the gelation bath side. This was found to be the case for several cellulose acetate casting solutions, including the acetone/formamide mixture of Manjikian. The surface tension of cellulose acetate in the latter mixture appeared to be much lower than in single solvents such as DMSO. The effects of surface tension were used to prepare asymmetric gels of poly(phenylene oxide) and nylon 11 by cooling high-temperature solutions in which γs 〉 γp at the gel transition point.
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  • 239
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    Journal of Applied Polymer Science 18 (1974), S. 2199-2203 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Additional Material: 3 Ill.
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  • 240
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    Journal of Applied Polymer Science 18 (1974), S. 727-734 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Permeability coefficients have been measured for normal butane, isobutane, isobutylene, and butene-1 in Zendel Copolymer-I at temperatures between 30° and 70°C and at penetrant pressures p1 up to 5.5 atm. The permeability coefficients of these organic vapors show behavior analogous to that observed for C3 and C2 hydrocarbons as detailed in our earlier work; i.e., near the condensation point of the penetrant, P increases as the temperature is decreased. Isothermal plots of log P versus p1 in that region are generally linear and can be represented by empirical relations of the form \documentclass{article}\pagestyle{empty}\begin{document}$$ P = P_0 \exp \left( {ap_1 } \right) $$\end{document} where P0 is a constant. The slope a is a function of temperature: \documentclass{article}\pagestyle{empty}\begin{document}$$ a = a_0 \exp \left( {bt} \right) $$\end{document} where a0 is a constant and b has the same value for the four hydrocarbons investigated.
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  • 241
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    Journal of Applied Polymer Science 18 (1974), S. 753-759 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: All isomers of phenanthrol, 1-, 2-, 3-, 4-, and 9-phenanthrol, were prepared and the inhibitory effect of these compounds on the thermal oxidative degradation of isotactic polypropylene was examined by conventional oxygen uptake. The phenanthrols were found to be much more effective antioxidants than commercial 2,6-di-tert-butyl-4-methyl-phenol (abbreviated as BHT), and phenanthrene itself hardly showed any inhibitive effect. The effect of the phenanthrols was largely dependent on the position of the hydroxy group; the order of the effect was as follows: 1- 〉 4- 〉 2- 〉 3- 〉 9-phenanthrol 〉 BHT. The phenanthrols were also good inhibitors of the radical polymerization of methyl methacrylate, and a fairly good correlation was observed between oxygen uptake and radical polymerization data.
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  • 242
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    Journal of Applied Polymer Science 18 (1974), S. 779-804 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Samples of low-density polyethylene, free from additives, were kept at temperatures between 284° and 355°C under nitrogen containing 1.16% oxygen or less. Changes in molecular weight distribution (MWD) and degree of long-chain branching (LCB) were followed by gel chromatography (GPC) and viscosity measurements. Other structural changes were investigated by infrared spectroscopy and differential scanning calorimetry (DSC). Both chain scission and molecular enlargement occur simultaneously. Chain scission accounts for the formation of low molecular weight material and volatiles. Molecular enlargement reactions cause an increase in LCB and ultimately the formation of insoluble material. At lower temperatures (284°C) an increase in the high molecular weight end of the MWD is observed. The amount of olefinic unsaturation, carbonyl, and ether groups increase with degradation. Conjugated systems are formed. The formation of thin discolored and insoluble surface layers indicate that the attack of oxygen is diffusion controlled. The DSC thermograms undergo large changes at 333° and 355°C, increasing with time and oxygen content. A reaction scheme for the thermo-oxidative degradation of polyethylene is discussed. Both inter- and intramolecular hydrogen abstractions by peroxy radicals are suggested to occur. Thus, the formation of trans-vinylene and ether groups results from intramolecular abstraction, while internal carbonyl groups are formed by intermolecular abstraction. Chain scission will be accomplished by both routes and together with “back-biting” is suggested to accoun for the formation of volatiles. The formation of conjugated sequences causing discoloration is correlated with the formation of trans-vinylene groups. Because of the restricted accessability of oxygen under our conditions, the reactions discussed previously for pure thermal degradation1 are also considered to be important. The molecular enlargement observed is thus proposed to be mainly due to the combination of alkyl radicals even when oxygen is present.
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  • 243
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    Journal of Applied Polymer Science 18 (1974), S. 867-886 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: CH2ClCH2Cl and CHCl3, in which bisphenol A polycarbonate is normally readily soluble, were sorbed into the polymer from the liquid phase at 24-25°C. Sorption behavior was studied over a range of solvent activities (ambient concentrations), and the effects of repeated sorptions were observed. Penetration was strongly dependent on solvent concentration and on the previous history of the polymer. Time dependence was also observed, evidently associated with the rate of relaxation processes in the polymer surface since the effects increased logarithmically with solvent activity. Analysis of sorption curves, supplemented by DSC and density determinations, showed that the sorbed solvents caused a structural rearrangement (ordering) of the polymer when present above the critical content of 0.3 w/w. The rearrangement was not identical with that caused by heating the polymer, as evidenced by differences in subsequent solvent sorption behavior.
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  • 244
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    Journal of Applied Polymer Science 18 (1974), S. 913-923 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Using a modified interfacial polymerization route, a graft copolymer of nylon 6,10 and polystyrene was prepared. First, an aqueous suspension of styrene monomer was encapsulated with nylon 6,10, followed by polymerization of the styrene to form the graft copolymer. When the material was subsequently molded below the crystalline melting point of nylon 6,10 (220°C), modulus-temperature behavior intermediate between polystyrene and nylon 6,10 was observed. However, when this graft copolymer was molded above the melting point of nylon 6,10, behavior more like pure polystyrene was observed. Phase contrast microscopy revealed that material molded below 220°C showed a continuous cellular-phase structure of about 30 microns in diameter, the interior of the cells being composed of polystyrene and the cell walls being composed of nylon 6,10. Phase inversion phenomenon was observed in the graft copolymer as the molding temperature was raised above 220°C. The nylon 6,10 phase became discontinuous, small globules being formed. This behavior is analogous to spheroidization in steel. It is thought that molten nylon 6,10 spheroidizes to attain a lower surface-energy state.
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  • 245
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    Journal of Applied Polymer Science 18 (1974), S. 963-974 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: In the presence of maleic anhydride-grafted polypropylene, marked dispersibility of the polymer blend of isotactic polypropylene and nylon 6 was obtained. This appeared to be caused by the formation of a certain graft polymer between maleic anhydride in polypropylene and terminal amino groups of nylon 6. The same phenomenon was observed when polystyrene and nylon 6 were blended with styrene-methacrylic acid copolymer as the interpolymer. The existence of such a graft polymer was confirmed by solvent extraction, estimation of the amino group of nylon 6, and identification by differential scanning calorimetry. The physical properties, especially mechanical properties of nylon 6-polypropylene polymer blends, were remarkably improved with increase of maleic anhydride added to the polymer blend. On the other hand, the physical properties those of nylon 6-polystyrene polymer blends were very little improved even in the presence of good dispersibility.
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  • 246
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    Journal of Applied Polymer Science 18 (1974), S. 1043-1052 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Epoxy resin was cured with diethylaminopropylamine (DEAPA) in amounts ranging from 10% to 50% of stoichiometric amount. The yield strength of resulting thermosets formed by heat curing at 75°C is found to increase with decreasing amount of hardener. This is attributed to a more densely crosslinked structure resulting from increased tertiary amine-initiated epoxide-epoxide chain reaction and decreased primary and secondary amine-epoxide reaction. Infrared analysis and swelling data are also presented. Styrene oxide diluent is found to have a moderate effect on mechanical properties in the range from 10 to 25 parts per hundred (phr).
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  • 247
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    Journal of Applied Polymer Science 18 (1974), S. 2517-2526 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Dehydrated castor oil (DCO) has been used as a comonomer with styrene to determine reactivity ratios. The polymerization was a free-radical process in benzene, and the product was isolated by evaporation of the reaction mixture and by two precipitations into petroleum ether from benzene. The copolymer composition was determined by a saponification procedure. DCO was found to have a high chain transfer constant and a very low reactivity ratio (estimated at 0.086) compared to styrene (11.6). It was found that copolymerization is difficult to achieve in a system where the DCO concentration in the reaction mixture was above 20 mole-%.
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    Journal of Applied Polymer Science 18 (1974), S. 2605-2610 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The prepolymer of diallyl isophthalate is employed as a material for a moistureprotective coating which is applied in the solution form, free of radical initiator. The effect of the absence of radical initiator, temperature and time of cure, and thickness of coat is evaluated in terms of the permeability of water through the protective films of the polyphthalate. Temperature of the noncatalytic cure can be as low as 170°C, and the presence of an initiator in the coating formulation does not bring about any improvement in the moisture resistance of the films.
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    Journal of Applied Polymer Science 18 (1974), S. 2569-2588 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: A study of a melt-spun threadline has been carried out to determine the effect of molecular weight on the elongational viscosity of the polymer being spun. Polymer chosen for this study was poly(ethylene terephthalate) having different molecular weights. Conventional nonisothermal spinning of the polymers was carried out with cooling by free convection. Threadline surface temperatures were measured by a null-balance technique. Threadline tension at the take-up device was measured, and samples of the threadline were taken to obtain linear density profiles. Nonlinear least-squares fits were applied to the linear density data to obtain equations for velocity and elongation rate. These measurements were then used to determine the threadline elongational viscosity. Least-squares fits were made to a polynomial relating absolute temperature and elongation rate to the elengational viscosity. These results were then used to determine an activation energy of elongational flow which was found to decrease with elongation rate. Elongational viscosity was found to increase with molecular weight.
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  • 250
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    Journal of Applied Polymer Science 18 (1974), S. 2671-2691 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The thermal decomposition of poly(oxypropylene) glycols was studied under nitrogen and dynamic operating conditions over the temperature range of 320° to 700°K by means of a differential scanning calorimeter. The differential energy losses due to changes in emissivity of the reference and sample pans were computed by modifying the baseline of the thermograms. Kinetic parameters obtained with the help of the Borchardt and Daniels theory indicate that the reaction is zero order and that the activation energy increases with molecular weight of the polymer. The rate of heating of the sample, the rate of flow of nitrogen, and the initial mass of the sample do not have significant effects on the kinetics of the decomposition.
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  • 251
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    Journal of Applied Polymer Science 18 (1974), S. 2725-2746 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Additional Material: 3 Ill.
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  • 252
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    Journal of Applied Polymer Science 18 (1974), S. 2785-2796 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Accessibility of wood adhesives was determined using a potassium bromide-embedding technique during resin cure. Cured resin was then extracted with water, followed by x-ray analysis of residual potassium bromide retention in the adhesive matrix. Cured urea-formaldehyde (UF), phenol-formaldehyde resol (PF), and phenol-resorcinol formaldehyde (PRF) accommodated large quantities of potassium bromide. However, only PRF adhesive showed crystallization of trapped potassium bromide, suggesting the presence of large pore sizes in the polymer lattices. Both UF and PRF adhesives, after room-temperature soaking, were equally resistant to water access. At higher temperature, water accessibility of UF increased greatly which may be attributed to thermal softening of the adhesive, while the accessibility of water to the PRF adhesive matrix was mainly a surface phenomenon and was not very temperature dependent. PF was highly accessible to water, even at room temperature, as a result of swelling from the presence of sodium hydroxide (catalyst). Accessibility of PRF adhesive was greatly increased by base (NaOH) solutions but not by acid (H2SO4) solutions. The UF resin showed slight increase of accessibility with increase in acidity and basicity of the water solution, but the accessibility increase of this adhesive in base solution was substantially less than that of PRF. The acid hydrolysis influence on accessibility increase of UF adhesive was far less severe than that of temperature.
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  • 253
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    Journal of Applied Polymer Science 18 (1974), S. 2829-2846 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The effects of polar parameter Σσ* and steric parameter ΣEs on reverse osmosis separations of alcohols, aldehydes, ketones, and ethers (noncyclic) in aqueous solutions involving single solute systems and porous cellulose acetate membranes are discussed. The least-squares and multiple-regression analyses of solute transport parameter data show that the separation of aldehydes, just as that of alcohols, is predominantly a function of Σσ*, and that of ethers is predominantly a function of ΣEs, whereas that of ketones is best represented as a function of both Σσ* and ΣEs. The results also indicate that even where water is preferentially sorbed at the membrane solution interface, solute separation in reverse osmosis is affected by the nonpolar character of the solute molecule. A general expression for solute transport parameter in reverse osmosis is presented for further study.
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  • 254
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    Journal of Applied Polymer Science 18 (1974), S. 2865-2874 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: A method for measuring the internal energy change of elastomers under compression is demonstrated using a conventional thermomechanical analyzer. The method is rapid and convenient and has a major advantage in that only a very small sample is required. Results are reported for natural rubber cured with two different crosslinking agents. The results are compared with previous work on similar materials in tension and torsion.
    Additional Material: 6 Ill.
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  • 255
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    Journal of Applied Polymer Science 18 (1974), S. 2927-2933 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The bulk and tap densities of a series of PVC resins were found to be related linearly to each other and hyperbolically to the resin specific surface.
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  • 256
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    Journal of Applied Polymer Science 18 (1974), S. 3445-3454 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Epoxy acrylates such as bisphenol type (I-A), propylene glycol type (II-A), and phthalic acid ester type (III-A) were prepared from addition reaction between each epoxy resin and acrylic acid. These reactions were carried out in the absence of solvent and in the presence of quaternary ammonium salt. The rate of addition reaction between glycidyl ether-type epoxide and acrylic acid obeyed first order. The rates of addition reaction between glycidyl ester-type epoxide and acrylic acid obeyed first order at 80°C, but obeyed second order rather than first order at 90°C and above. The rates of photocrosslinking of epoxy acrylates were measured by IR spectrophotometry. Epoxy acrylates with benzoin ethyl ether (1 wt-%) were irradiated with a high-pressure mercury lamp in oxygen-free atmosphere. The rates of photocrosslinking of epoxy acrylates II-A, III-A, and I-A decrease in that order.
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  • 257
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    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The addition of mercaptoethanol and hydrogen sulfide to the pendent double bonds of acrylamidomethylated cotton (AMC) has been investigated. The interaction of acrylonitrile with the modified celluloses so obtained (substrate I and II) and with AMC treated with ammonium hydroxide (substrate III) in the presence of Ce(IV) is studied. Substrate I shows higher initial grafting yields. than AMC; the opposite holds true for the maximum graft yields. The graft yields obtained with substrate II are lower than those of AMC. All modified cottons studied are less amenable to grafting compared with the unmodified cotton. The graft yields of AMC and substrate III are comparable due to the fact that both substrates are crosslinked. Probable reasons for the inferior reactivity of substrates I and II are also given.
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  • 258
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    Journal of Applied Polymer Science 18 (1974), S. 2095-2115 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: A study has been made of the reaction products of hydroxymethylated 2-substituted (X) 4,6-diamino-s-triazines (MXT) with cotton fabrics in the presence of zinc nitrate as catalyst. The reagents used were MXT having the following substituents: methoxy (MMT), isopropoxy (MIPT), methyl (acetoguanamine) (MAG), monoethylamino [N-(2-ethyl)melamine] (MEM), monohydroxyethylamino [N-(2-hydroxyethyl)melamine] (MHEM), and dihydroxyethylamino [N,N-bis(2-hydroxyethyl)melamine] (MBHEM) groups. Trimethylolmelamine (TMM), dimethylolurea (DMU), dimethylolethyleneurea (DMEU), and dimethylolethyltriazone (DMET) were also used for comparison.The molar ratio of total formaldehyde to 2-substituted 4,6-diamino-s-triazine (XT) residue in treated fabrics is larger in high-temperature curing than in low-temperature curing. In case of curing at 150°C for 5 min, MHEM and MBHEM crosslinked primarily with cellulose in a monomeric state, and the others in a oligomeric state. From these facts, the crosslinked structures were presumed. Infrared absorption spectra of the fabrics treated with MXT are discussed and a few physical properties of the fabrics are compared with those of the fabrics finished with TMM, DMU, DMEU, and DMET.
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  • 259
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    Journal of Applied Polymer Science 18 (1974), S. 2379-2390 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: For batch emulsion polymerizations of vinyl chloride, the reaction rate can be well represented by the empirical expression dx/dt = k (1 + ax), where x is the polymer concentration, and k and a are constants dependent upon initiator concentration and particle number. A simple mathematical model for continuous stirred-reactor polymerizations has been derived from this expression. The model predicts that at short residence times, a steady state of low PVC concentration is reached quickly; with longer residence time, the system more slowly approaches a higher steady-state polymer concentration. Above a critical residence time, equal to 1/ak, the rate of monomer supply becomes the limiting factor. Experimental data on continuous polymerizations are in good qualitative accord with the predictions of the model using constants fitted to batch-charge data. Quantitative agreement is best when the particle number is large; discrepancies may be attributed to a broader particle size distribution in continuous runs. Particle size measurements show evidence of intermittent particle formation in unseeded continuous runs; continuous seeding narrows the particle size distribution, but it is still broader than in batch charges. The model seems sufficiently valid to yield a number of useful implications about practical aspects of continuous emulsion PVC polymerization.
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  • 260
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    Journal of Applied Polymer Science 18 (1974), S. 2539-2568 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: An experimental study of the spinnability and the variation in crystallinity and orientation in high-density and low-density polyethylene fibers with melt spinning and drawing conditions has been carried out. Three polymers (two high-density and one low-density) and eicosane (C20H42) were studied. The maximum spinnability was in the lower molecular weight high-density polyethylene. Hermans-Stein a, b, and c crystallographic axis orientation factors were computed from wide-angle x-ray scattering patterns. In the spun fiber, small take-up velocities cause the b axis to become perpendicular to the fiber axis in each fiber. The c axis increasingly orients itself parallel to the fiber axis as take-up velocity increases. The a axis orientation is different for each polymer. The results are interpreted in terms of modern theories of crystalline morphology, specifically the development of row structures. In the drawing experiments, the two high-density polyethylenes necked. A phenomenological theory of necking is discussed. The a, b, and c axis orientation factors were determined for different stages of drawing. In the necked regions and in completely drawn fibers, the c axis was parallel to the fiber axis and the a and b axes are perpendicular to the fiber axis. The tangent Young's modulus and tensile strength of the spun fibers increased with take-up velocity and in the drawn fibers were an order of magnitude higher than in the spun fiber. The mechanical properties of spun fiber may be correlated with the c axis (Hermans) orientation factor. The drawn fiber shows significant variations in Young's modulus and tensile strength at constant unit cell orientation.
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  • 261
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    Journal of Applied Polymer Science 18 (1974), S. 2623-2636 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Chemisorption and crosslinking of cotton cellulose has been carried out with DMEU, DMPU, DHEU, and DMDHEU. Various physicochemical properties of resin-treated samples have been studied and the data subjected to a linear regression analysis. Using the techniques of liquid retention and optical microscopy it has been found that the chemisorbed cotton is characterized by a lower level of bound resin, greater amount of methylol HCHO, and higher swellability of structure in comparison to the crosslinked cotton. This difference of behavior between the two cottons is attributed to greater rigidification and a collapse of porous structure in crosslinked cotton as a result of catalytic activity at the curing temperature. For various resin-treated samples there exists a linear relationship between the strength and recovery characteristics of single fibers and those of fiber bundles. The losses in fiber strength and extensibility are found to be proportional to the level of bound resin in various samples. Crosslinked fibers show appreciably higher magnitudes of elastic recovery and bundle crease recovery than chemisorbed fibers. The significance of these results is discussed.
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  • 262
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    Journal of Applied Polymer Science 18 (1974), S. 3237-3247 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The adhesion of low-density polyethylene to porous anodic films on aluminum was studied using the 180° peel test. Relative values of bond strengths, obtained by using polymer with and without antioxidant and by forming the bond in air or in vacuo, indicated that good adhesion could be obtained, despite previous evidence to the contrary, in conditions where oxidation of the polyethylene was suppressed. The relation between peel strength and anodic film thickness and film-forming voltage implied that the polyethylene entered pores in the film during bond formation. This was supported by the change of the category of the adhesion to one dependent upon polymer oxidation when the pores in the anodic film were sealed prior to bond formation. It is suggested that the mechanism of adhesion to porous anodic films on aluminum involves keying of the polymer into the pores in the film.
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  • 263
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    Journal of Applied Polymer Science 18 (1974), S. 3259-3266 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: A silicon-substituted azonitrile, has been synthesized by the hydrosilation of 5-hexene-2-one azine with methyldichlorosilane in the presence of chloroplatinic acid, followed by hydrocyanation with anhydrous HCN, and subsequent oxidation with chlorine. The azonitrile is an initiator for radical polymerizations. It is especially useful for the preparation of low molecular weight polymers that, after treatment with acetic anhydride, cure at room temperature in the presence of atmospheric moisture. The preparation of a series of room temperature- vulcanizable materials based on a tetrafluoroethylene/methyl vinyl ether copolymer is described.
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  • 264
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    Journal of Applied Polymer Science 18 (1974), S. 3311-3318 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The latex-suspension technique is used to prepare a family of rubber-modified polystyrene resins possessing high-impact resistance (Izod ca. 1.5 ft-lb/in.), high gloss, high heat distortion temperature, and high tensile properties. Data are presented on the preparation of medium- and low-impact grades by physical blending with crystal polystyrene and on the preparation of ultrahigh-impact polystyrene (Izod ca. 3.5 to 6) through the incorporation of high concentrations of rubber made feasible by the latexsuspension process.
    Additional Material: 3 Ill.
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  • 265
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    Journal of Applied Polymer Science 18 (1974), S. 53-59 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Synthesis of zirconium oligomeric polythioethers was effected using aqueous solution and interfacial techniques: The products are insoluble in all tried solvents and possess Zr—OH endgroups but no detectable quantities of R—SH, Zr—Cl, or Zr—N—Et-endgroups.
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  • 266
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    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: In a previous paper1 it was mentioned that trapped radicals in poly(maleic anhydride) (Poly-MAH) have the ability to initiate cationic polymerization. In this paper, the cationic polymerization of isobutyl vinyl ether (IBVE) is described using Poly-MAH as the initiator. These radicals show different behavior during polymerization depending upon their structure. In particular, large conjugated radicals initiate ionic polymerizations.
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  • 267
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    Journal of Applied Polymer Science 18 (1974), S. 167-178 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Critical surface tension values γc were measured for poly(n-alkyl methacrylates) and copolymers of stearyl methacrylate with methacrylonitrile. Surface tension values γL of n-alkyl methacrylate increase with increasing side chain length: γL = 23.2 dynes/cm for methyl methacrylate to 33.2 dynes/cm for stearyl methacrylate, but γc values of poly(n-alkyl methacrylate) decrease with increasing side chain length: γc = 36.3 dynes/cm for poly(methyl methacrylate) to 20.8 dynes/cm for poly(stearyl methacrylate). The decrease in γc is attributed to a tighter packing of the alkyl chain with a greater concentration of the pendent —CH3 group at the air/solid interface. Values of γc of copolymers hardly depended on the methacrylonitrile content in copolymers and did not satisfy the equation γc = N1γc1 + N2γc2 proposed by Lee. The difference in γc values for casting, annealing, and quenching films of poly(stearyl methacrylate) and the surface structure of copolymers were discussed using electron microscopy and measurement of melting point, heat of melting, and γc.
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  • 268
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    Journal of Applied Polymer Science 18 (1974), S. 235-243 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Exposure of polyethylene film to UV radiation at wavelengths of ≤2537 Å is sufficient to induce surface crosslinking and to facilitate the formation of strong adhesive joints to these surfaces with conventional adhesives. Reduction of the vapor pressure in the reaction vessel to about 1 torr apparently maximizes the efficiency of the crosslinking process. Examination of the treated films which have been exposed for times necessary to form strong adhesive joints has revealed an absence of surface oxidation. It appears that crosslinking to improve the mechanical strength of the surface region of the polyethylene is sufficient to allow the formation of strong adhesive joints.
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  • 269
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    Journal of Applied Polymer Science 18 (1974), S. 1-20 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Five methods were modified to test for interactions between binder and filler of composite solid propellants. Methods based on uncured binder or model compounds were rate of solution of binder from composite mixtures; centrifugal separation of binder from the filler; of composite mixtures; measurement of the contact angle between binder and filler; and adsorption of binder or model compounds by filler from solution. Stress-strain-birefringence was measured on cured binders containing small amounts of filler. In addition to the polymers used as binders and the model compounds, three physical forms of aluminum, and the additives tris [1-methylaziridinyl] phosphine oxide (MAPO) and a polysebacate of methyl-N-diethanolamine were included in the study. The filler was ammonium perchlorate in all experiments. The polysebacate was an effective adhesion improver in the polyurethane-ammonium perchlorate composite. MAPO was not as effective in the system polybutadiene-ammonium perchlorate. Fibrous forms of aluminum result in a weaker propellant then does powdered aluminum. Nonfunctionally terminated polymers were poorer in adhesion, contact angel, and adsorption tests compared with carboxyl- and hydroxyl-terminated types. The nonpolymeric model compounds yielded inconclusive data.
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  • 270
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    Journal of Applied Polymer Science 18 (1974), S. 77-82 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The design and operation of an automated density balance are outlined. Diverse uses for this equipment are discussed.
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  • 271
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    Journal of Applied Polymer Science 18 (1974), S. 193-202 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: A method is outlined for estimation of small degrees of long-chain branching in polymers with moderately narrow molecular weight distribution (M̄w/M̄n 〈1.4). The storage and loss shear moduli, G′ and G″, are measured in dilute solution by the Birnboim-Schrag multiple-lumped resonator and extrapolated to infinite dilution, choosing a suitable solvent viscosity and frequency range such that the data lie in the terminal zone where G′ and G″ are proportional to the second and first powers of frequency, respectively. The intrinsic reduced steady-state shear compliance is determined from these data and corrected for moderate molecular weight heterogeneity (assuming a Gaussian distribution) from knowledge of M̄w/M̄n and the Mark-Houwink exponent a. The resulting value of S2/S12 (where S1 = Στp/τ1, S2 = Σ(τp/τ1)2, the τp's being the relaxation times and τ1 the longest one) is compared with values calculated by the Zimm-Kilb theory as evaluated by Osaki for comb polymers of regular geometry and different numbers of branch points. The method has been illustrated by measurements on four ethylene-propylene copolymers. One containing no termonomer and one containing a saturated termonomer appeared to be linear; two containing unsaturated termonomers showed small degrees of branching. The method appears to be promising for detecting from one to four branch points per molecule.
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  • 272
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    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Viscoelastic fatigue studies were made on poly(vinyl chloride) (PVC) films using oscillatory loading on prestressed samples in an ethanol vapor environment. Samples include unfractionated PVC, relatively narrow molecular weight distribution fractions, and blends made from the fractions. Strain, complex modulus, and tan δ were studied as a function of time until rupture occurred. A marked dependence on molecular weight was observed, for example, a fraction with M̄w = 51,000 failed in a few seconds, while one with M̄w = 228,000 did not fracture after 1600 min.
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  • 273
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    Journal of Applied Polymer Science 18 (1974), S. 267-291 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The fatigue properties of a number of different types of fibers have been investigated and failure under cyclic loading conditions compared to that caused by simple tensile loading. Polyamide, polyester, and polyacrylonitrile fibers have been studied and all have been found to fail by fatigue mechanisms. The loading conditions have been monitored by a fiber fatigue apparatus developed for this purpose and the fracture morphologies inspected by scanning electron microscopy. In all of the cases which are considered in detail, fatigue failure of the fibers has been found to occur when cycling from zero load to a maximum load of about 60% of the tensile strength. Fatigue failure is accompanied by a distinctive fracture morphology, clearly different from the tensile fracture morphology and involving crack propagation along the fiber at a slight angle to its axis, although the mechanism which causes this in the acrylic fiber is probably different from that for the polyamide and polyester fibers.
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    Journal of Applied Polymer Science 18 (1974), S. 317-317 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
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  • 275
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    Journal of Applied Polymer Science 18 (1974), S. 343-349 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The bond strength of an amine-cured epoxy resin to etched aluminum washed with, or washed with and immersed in, 10°C tap water was found to be greater than joints similarly pretreated in 10°C distilled water. The higher bond strength was found to be induced by soluble cations of less than 0.8 Å radius; larger cations had no effect. When aluminum is etched in a solution of chromic acid at 65°C, the aluminum surface is oxidized to γ-Al2O3. It is possible that the small, soluble cations can occupy the cationic vacancies in the defect spinel structure of the γ-Al2O3 and reduce the negative charge on the surface of the aluminum joints. Joints pretreated in 60°C tap water exhibited higher bond strengths than those pretreated in 60°C distilled water, as the growth of a thick, weak layer of bayerite was inhibited by large anions present in the tap water.
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  • 276
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    Journal of Applied Polymer Science 18 (1974), S. 567-588 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Reverse osmosis transport for alcohol-water systems in the Taft number (σ*) region of 0 to -0.3 is explored in detail. The numerical value of the polar functional constant for alcohols is 15.5 for the above σ* region in the operating pressure range of 50 to 500 psig for the cellulose acetate membrane material used. An analysis of the combined effect of operating pressure and mass transfer coefficient on the high-pressure side of the membrane shows that, under certain conditions, solute separation could pass through a maximum with increase in operating pressure. A general experession for solute separation is derived as a function of pore structure on membrane surface, polarity of solute, and operating conditions of the experiment. Alcohols behave independently in mixed solute systems. A method is described and illustrated for predicting alcohol separation in alcohol-sucrose-water feed solutions from data on single solute systems.
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  • 277
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    Journal of Applied Polymer Science 18 (1974), S. 615-623 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Crystallization during melt spinning is studied as an example of the nonisothermal crystallization of polymers. The following equation is derived, taking the temperature distribution within a filament into consideration: \documentclass{article}\pagestyle{empty}\begin{document}$$ \kappa \nabla ^2 T = {\rm V} \cdot {\rm grad } \ T - \frac{{\Delta H}}{{C_p }}{\rm V} \cdot {\rm grad } \ X $$\end{document} where T = temperature, X = crystallinity, κ = thermal diffusivity, V = velocity, ΔH = heat of crystallization, and Cp = specific heat at constant pressure. The assumptions and the procedure for a numerical calculation of crystallinity and temperature within a running filament are described, and some results of calculation are illustrated. The results are compared with those obtained by a simpler calculation in which the radial temperature distribution is neglected. The simpler method proved useful in connection with x-ray measurements.
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  • 278
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    Journal of Applied Polymer Science 18 (1974), S. 671-674 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Assuming the applicability of the Arrhenius equation to the polycondensation processes, two-by-two homopolycondensation processes proceeding with one of the monomers - the same in both cases - were examined. It was considered whether there is a temperature at which the reactivity of the two different monomers becomes the same. The isokinetic temperatures for four different systems were determined experimentally, and it was found that they are within an accessible experimental range.
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  • 279
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    Journal of Applied Polymer Science 18 (1974), S. 699-708 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The diffusion coefficient of a solvating liquid or vapor in a semicrystalline membrane can be measured in a number of ways. In a previous paper, we discussed methods based on permeation rates. Here, we consider sorption-desorption kinetics at near-ambient temperatures. Anomalies are identified and possible causes discussed in the light of new experiments, mostly involving p-xylene and polyethylene.
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  • 280
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    Journal of Applied Polymer Science 18 (1974), S. 735-744 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Laser Raman spectroscopy was used to monitor changes in the substitution pattern during the formation of a phenol-formaldehyde resin (resol). The substitution-sensitive bands were identified and their relative intensities related to molecular weight of the resol. Results of this study are similar to those obtained by previous workers in the field using paper chromatography. The absorbance ratio of 784-cm-1 to 998-cm-1 bands was found to be linearly related to the molecular weight of the resol.
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  • 281
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    Journal of Applied Polymer Science 18 (1974), S. 821-829 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: An experimental study was carried out to investigate the viscoelastic behavior of calcium carbonate-filled polypropylene melts, using the Han slit rheometer. In the analysis of the experimental data, the pressure gradient was used to determine the wall shear stress, and the exit pressure to determine the elasticity of the filled polymers. The study shows that the materials studied follow a power law in viscous behavior over the range of shear rates investigated and that the viscosity increases and elasticity decreases as filler concentration is increased. Also investigated was the effect of temperature on the viscoelastic properties of filled polypropylene melts.
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  • 282
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    Journal of Applied Polymer Science 18 (1974), S. 843-856 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: As an aid in assessing the ability of antioxidant additives to persist in polymers and thus remain effective in protecting against oxidation, the solubility and diffusion coefficient of two antioxidants in branched polyethylene have been determined in this work. A method was developed for this purpose by which the diffusion coefficient and solubility could be determined simultaneously. The method consists of analyzing the concentration profile across a stack of polyethylene sheets through which the antioxidant was allowed to diffuse. The concentration of antioxidants in polyethylene was determined by a thermogravimetric technique which relies directly on the ability of the additives to suppress oxidation reaction. The diffusion coefficients determined showed excellent agreement with values in the literature which were obtained by a radiotracer method. The solubility of the antioxidants in three normal hydrocarbon solvents of varying molecular sizes was also determined by a conventional technique at various temperatures and found to correlate well with their solubility in polyethylene determined by the diffusion method. In particular, the dependence of the solubility on the size of solvent molecules and on temperature agrees well with an equation derived on the basis of the regular solution theory of liquid mixtures.
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  • 283
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    Journal of Applied Polymer Science 18 (1974), S. 1351-1358 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The hypothetical fractionation of polyethylene-polypropylene blends was carried out by assuming adequate molecular weight distribution and partition of polymer between two liquid phases for each hompolymer, and also by using the previously reported data of the molecular weight dependence on solubility. The experimental fractionation of blends was also carried out by the solvent gradient method, and the results were compared with those obtained by the hypothetical fractionation. Both results agreed fairly well in various distribution forms. Therefore, these results may provide valuable information for component or compositional analysis of unknown samples or copolymerization products.
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    Journal of Applied Polymer Science 18 (1974), S. 1407-1410 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The kinetics of the reaction between urea and formaldehyde were studied in the presence of various amounts of sulfuric acid (5-45% by weight) at different temperatures (5°, 15°, and 25°C). The reaction was shown to follow first-order kinetics. The activation energy for the reaction varies from 12.51 kcal/mole to 14.59 kcal/mole in the range of sulfuric acid concentration studied.
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  • 285
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    Journal of Applied Polymer Science 18 (1974), S. 1433-1441 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: This work used a conventional thermomechanical analyzer (TMA) to measure the depth of indentation at room temperature of elastomers and Finkin's equation to calculate Young's moduli of elastomers, which have been measured by Drutowski, from the radius of contact of an indentor on thin sheets of sample. Data obtained from the TMA are compared with those measured by radius of contact and Hertz contact theory and are found in good agreement. Measurements of Young's modulus as a function of temperature at different heating rates by TMA were made for an acrylic elastomer. The results are compared with theory and the deviations from theory are discussed.
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    Journal of Applied Polymer Science 18 (1974), S. 133-142 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Water-soluble films of cellulose nitrate-nitrite were prepared by dissolving bleached sulfite pulp in a solution of nitrogen dioxide in dimethylformamide (DMF) at room temperature and heating the solution at 70°C for about 3 hr. Their water sorption, fine structure, and electrical properties were measured and compared with those of three other films - one water soluble (poly(vinyl alcohol)) and two water insoluble (cellophane and a film prepared from a cellulose solution in the nitrogen dioxide-DMF mixture and cast immediately after the cellulose had dissolved at room temperature). A comparison between the properties of water-soluble films and the poly(vinyl alcohol) film showed that the former had higher crystallinity, lower moisture absorption in the 0-80% relative humidity region, lower permittivity and a.c. conductance, and higher d.c. resistance. The DMF-cast water-insoluble film adsorbed less moisture than the cellophane film.
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  • 287
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    Journal of Applied Polymer Science 18 (1974), S. 1541-1548 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Kinetic information on the resinification of furfuryl alcohol has been derived from the rate of increase of color intensity measured with a photoelectric colorimeter, the resinification being carried out isothermally in Clark-Lubs aqueous buffer solutions in the pH range of 1.0-2.2. The activation energy for polymerization is found to increase exponentially with pH. The time required for emulsification (which is quickly followed by separation of resin layer) to occur in an aqueous solution of furfuryl alcohol also increases exponentially with pH, but it decreases exponentially with temperature. This is described quantitatively by a single expression.
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    Journal of Applied Polymer Science 18 (1974), S. 1557-1574 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The adhesion of poly(ethylene terephthalate) (PET) to rubber in tire composites was significantly improved by exposure of the PET to “low-temperature” gas plasmas. Rubber composites built using a single-dip resorcinol-formaldehyde-latex (RFL) adhesive and plasma-treated PET reinforcement were studied. The effects of treatment conditions on this adhesion improvement were examined. The improvement was insensitive to nature of the gas, exposure time, power level, and pressure within the operating limits of the plasma generator. Fiber finish on filaments being treated was detrimental to the adhesion improvement; however, an overcoating of treated filaments with finish was not detrimental. The effects of tire building operations on this adhesion improvement of treated PET were examined. The improvement was found over a wide range of adhesives, adhesive-curing conditions, rubber compositions, and bonding testing conditions.
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    Journal of Applied Polymer Science 18 (1974), S. 1587-1602 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The melting phenomena of aqueous polymer solutions and gels have been investigated by differential scanning calorimetry (DSC). The polymers used were synthetic polyacrylamide and poly(vinyl alcohol) samples as well as guar and xanthan gums. By using an empirical relation, the energy measured from the area under the melting peak yielded heats of mixing and sorption, when fitted by an association factor computed from the data. This factor (independent of the concentration) is a measure of the water fraction associated with the polymer and has a definite and characteristic value for a given polymer in water. When a crosslinking agent (potassium pyroantimoniate or chromic nitrate) was added to the water-polymer system, the association factor varied with the polymer concentration; the macromolecular chains thus become less accessible to penetrating water. If a branched gel was obtained owing to the formation of chemical crosslinks, a hump appeared on the melting peak.
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  • 290
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    Journal of Applied Polymer Science 18 (1974), S. 1693-1709 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: This paper describes an interfacial viscometer. Rheological data of polymeric surfactants were obtained with the use of the instrument for liquid-liquid and liquid-gas interfaces. The surfactants studied were methylcellulose, poly(vinyl alcohol), polymer of diethylene glycol n-butyl ether acrylate, and sulfonated poly(vinyltoluene). Investigations were conducted over a wide range of temperatures and concentrations of the surfactants in the liquid phase. The instrument was used to obtain surface area coverage data for the surfactants studied. The experimental data were compared with theoretical calculations. The data indicated that the absorbed film at the interface was an irregular film, i.e., not an ordered packing of the molecules at the interface. Significance of interfacial viscosity on droplet break-up in a simple shear field was investigated. Droplet breakup studies substantiate the hypothesis that an absorbed polymeric film at an interface forms a complex viscous film.
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    Journal of Applied Polymer Science 18 (1974), S. 2221-2227 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: By using the method of scanning electron microscopy, a visual study was made of the macro-deformation of spherulitic deformation during the cold rolling of poly(ethylene terephthalate) (PET) and poly(tetramethylene terephthalate) (PTMT). By rolling solution cast films to different extension ratios, it was found that the surface material (nearest the rollers) appeared to deform first by the shearing action. With higher extension, the material toward the core of the film began to deform. In all cases, the deformation process tended to flatten the spherulites yet, in general, the spherulitic boundaries were maintained. It was noted that the same general behavior was observed for both PET and PTMT.
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  • 292
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    Journal of Applied Polymer Science 18 (1974), S. 2261-2268 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The spherulitic structure of films of fractionated bisphenol-A-polycarbonate having a range of different average molecular weight and molecular weight distribution has been studied using the polarization microscope. Spherulitic crystallization was induced in specimens by the action of solvent or solvent vapor at room temperature or by isothermal heat treatment at 180°C. These phenomena were all shown to be a function of the average molecular weight and polydispersity of the material. The glassy amorphous and spherulite polymer phases were investigated using a microscopic etching technique and gel permeation chromatography (GPC). Results of this investigation have established that considerable segregation by molecular weight occurs during the crystallization process. Spherulites produced have been shown to exhibit variation in morphologic texture depending on conditions of induction and polydispersity of the polymer. Examples of unusual and previously unreported spherulites have been observed.
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    Journal of Applied Polymer Science 18 (1974), S. 2307-2310 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: A number of block and graft copolymers have been prepared from several vinyl monomers, and their glass transition temperatures measured. The series included polar, nonpolar and polar-nonpolar pairs. It was found in all cases except one that the glass transition temperatures were close to those found for the individual homopolymers. The exception was a block copolymer of styrene and α-methylstyrene, the only pair whose homopolymers would give clear mixed solutions in a mutual solvent.
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    Journal of Applied Polymer Science 18 (1974), S. 2339-2353 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The tearing energy theory developed to describe the failure properties of vulcanized rubbers is shown to be applicable to the cut growth and fatigue properties of cellular polyurethanes. The effective inherent flaw size to initiate cut growth in the cellular polyurethane predicted from fatigue results has been found to be similar to the measured size of the largest pore in the material. The cut growth properties of the cellular polyurethane have been compared with solid polyurethane of the same type, crosslinked polyurethanes, and vulcanized rubbers. It is found that the minimum value of tearing energy (T0) under which no fatigue failure occurs in the absence of chemical effects is far higher in polyurethanes than vulcanized rubbers. It is thought that this is due to the segmented structure of the polyurethane which has highly hysteresial tensile properties.
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    Journal of Applied Polymer Science 18 (1974), S. 2391-2397 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The Q-factors for ten poly-1-olefins from poly-1-butene to poly-1-octadecene were determined in 1,2,4-trichlorobenzene at 80°C and 135°C using the universal calibration curve and the elution count-extended chain length calibration curve constructed by use of polystyrene standards. These experimentally determined Q-factors were lower than the theoretical ones, except for poly-1-butene, at both temperatures, in contrast to those for polyethylene, polypropylene, and poly-1-butene. Corrected Q-factors for poly-1-olefins were obtained by correlating apparent Q-factors with the number of carbon atoms in the monomer for a series of poly-1-olefins. By assuming that poly-1-olefins in solution exist as quasi-rod-shaped polymers rather than random coils, it would be presumed that the apparent extended chain lengths of poly-1-olefins experimentally determined are longer than the theoretical ones because of the effects of their long pendent groups which influence the elution positions of poly-1-olefins. A molecule of the poly-1-olefins having the same theoretical extended chain length of a polystyrene molecule elutes earlier than the polystyrene molecule, meaning the extended chain length of the poly-1-olefin molecule is supposed to be longer than that of the polystyrene molecule.
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    Journal of Applied Polymer Science 18 (1974), S. 2449-2455 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: 2,4-Dinitrophenylhydrazine was reacted on polyethylene films irradiated in air with ultraviolet light. The changes in amount of carbonyl groups and 2,4-dinitrophenyl-hydrazones formed in the films were inferred by comparing their absorptions in the infrared and ultraviolet spectra, respectively. The amount of hydrazones formed increased with increase in the reaction time, and rates of the increase gradually decreased with increase in the reaction time. A comparison of the change in amount of hydrazones formed in the irradiated films with the change in amount of carbonyl groups formed in the irradiated films and the change in wettability with H-bonding liquids of the irradiated films showed that the amount of hydrazones formed seemed to be affected by amount of carbonyl groups in the surface zone of the film. The carbonyl groups were regenerated from the hydrazones with increase in the regeneration times, and rates of the regenerations gradually decreased with increase in the regeneration times. The regeneration was facilitated by raising the temperature in the levulinic acid solution, by adding dilute hydrochloric acid to the levulinic acid, or by raising the temperature in the levulinic acid solution containing hydrochloric acid.
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    Journal of Applied Polymer Science 18 (1974), S. 2287-2306 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Der Einfluß von Zusatzstoffen auf die Werkstoffeigenschaften von Hochdruck-Polyäthylen wird mit Glaskugeln und Quarzmehl, Talk und Glimmer sowie Asbest-und Glasfasern untersucht. Die eingemischten Materialien erhöhen die Steifigkeit, die Festigkeit sowie die Härte und erniedrigen die Reißdehnung, die Schwindung und verschlechtern das Fließverhalten des Grundwerkstoffs. Die Wirkung der Zusatzstoffe wird durch die zugängliche Grenzfläche nnd die Haftstellendichte der Makromoleküle an der Grenzfläche bestimmt. Daher ist neben der chemischen Zusammensetzung, die Geometrie des Zusatzstoffes eine wesentliche Einflussgröße. Die experimentellen Ergebnisse der relativen E-Modulerhöhung von Teilchenverbunden stimmen für Konzentrationen bis 40 Gewichtsprozent mit theoretischen Voraussagen gut überein.
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    Type of Medium: Electronic Resource
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  • 298
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 18 (1974), S. 2457-2464 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: In the radiation-induced emulsion copolymerization of tetrafluoroethylene with propylene, it was found that hydrofluoric acid (HF) is formed in the course of polymerization. The amount of HF formed increased linearly with the irradiation time in all cases. The rate of HF formation was maximum at 0.3 wt-% emulsifier and increased linearly with tetrafluoroethylene content in the monomer mixture. On the other hand, the conversion and the molecular weight decreased remarkably by addition of 0.1M HF. The particle diameter of copolymer obtained in the presence of HF was larger than that obtained in the HF-free system. On the contrary, the number of polymer particles was less than that obtained in the HF-free system. The decrease in the conversion and the molecular weight was attributed mainly to the conversion of part of ammonium perfluorooctanoate to perfluorooctanoic acid by formation of acid or addition of acid.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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  • 299
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 18 (1974), S. 1243-1245 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 300
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 18 (1974), S. 1265-1267 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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